NDC 43617-3415 Lanocreme Hydrating Day Spf15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43617-3415?
Which are Lanocreme Hydrating Day Spf15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Lanocreme Hydrating Day Spf15 Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- TRICAPRYLIN (UNII: 6P92858988)
- TRICAPRIN (UNII: O1PB8EU98M)
- SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LANOLIN (UNII: 7EV65EAW6H)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW) (UNII: 2WID9OCG7P)
- EDETATE SODIUM (UNII: MP1J8420LU)
- KIWI FRUIT (UNII: 71ES77LGJC)
- HONEY (UNII: Y9H1V576FH)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".